BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SOL 13.5 STD 8.0 FULL PC 12/14

    MDR report key: 1895044 · Received November 5, 2010

    Report

    Report Number
    1818910-2010-07905
    Event Type
    Injury
    Date Received
    November 5, 2010
    Date of Event
    October 8, 2010
    Report Date
    October 8, 2010
    Manufacturer
    DEPUY ORTHOPAEDICS, INC.
    Product Code
    LPH
    PMA / PMN Number
    K953703
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

    Description of Event or Problem · 1

    PATIENT REVISED FOR FRACTURED STEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SOL 13.5 STD 8.0 FULL PC 12/14 87 LPH LPH DEPUY ORTHOPAEDICS, INC. NA VD9BB1005

    Patients

    Seq Age Sex Outcome Treatment
    1 71 YR Required Intervention